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Jintao Hu, Qingbo Chen, Xiao Ding, Xin Zheng, Xuefeng Tang, Song Li, and Hui Yang

Background Pituitary adenoma (PA) is the second most common brain tumor. Except for prolactinoma, pituitary tumors associated with acromegaly (growth hormone-secreting) and Cushing’s disease (adrenocorticotropic hormone-secreting) as well as

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Marília D’Elboux Guimarães Brescia, Karine Candido Rodrigues, André Fernandes d’Alessandro, Wellington Alves Filho, Willemijn Y van der Plas, Schelto Kruijff, Sergio Samir Arap, Sergio Pereira de Almeida Toledo, Fábio Luiz de Menezes Montenegro, and Delmar Muniz Lourenço Jr

(prolactinoma, 9; acromegaly, 1; non-functioning tumor, 8) being 1 case operated 2 months after PTx by non-functioning while other waited surgery for acromegaly performed more 1 year after PTx. A pancreatectomy by pancreatic NET had been performed previously in

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Alessandro Brancatella and Claudio Marcocci

of fracture, independently from BMD ( 36 , 37 ), as often seen in some endocrine disorders, namely acromegaly, Cushing’s disease, hyperparathyroidism and hyperthyroidism ( 38 , 39 , 40 ). Another classical example is glucocorticoid

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Rossella Cannarella, Andrea Crafa, Sandro La Vignera, Rosita A Condorelli, and Aldo E Calogero

Introduction The acromegaly levels of insulin-like growth factor 1 (IGF1) that occur in healthy children in pubertal age have led to the speculation that this hormone may stimulate the function of the hypothalamus–pituitary–testicular (HPT

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Filippo Ceccato, Elisa Selmin, Giorgia Antonelli, Mattia Barbot, Andrea Daniele, Marco Boscaro, Mario Plebani, and Carla Scaroni

. ACTH deficiency, higher doses of hydrocortisone replacement, and radiotherapy are independent predictors of mortality in patients with acromegaly . Journal of Clinical Endocrinology and Metabolism 2009 94 4216 – 4223 . (

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Yu Lin, Yingying Zhang, Lei Xu, Wei Long, Chunjian Shan, Hongjuan Ding, Lianghui You, Chun Zhao, and Zhonghua Shi

, pheochromocytoma, acromegaly, history of smoking, chemical dependency, use of assisted reproductive technology, multiple gestation, and any other confounding pathologies, including hyperthyroidism and hypothyroidism. The exclusion criteria for infants were as

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Danielle Christine Maria van der Kaay, Anne Rochtus, Gerhard Binder, Ingo Kurth, Dirk Prawitt, Irène Netchine, Gudmundur Johannsson, Anita C S Hokken-Koelega, Miriam Elbracht, and Thomas Eggermann

. ( ) 10.1159/000081063 32 Dahlqvist P Spencer R Marques P Dang MN Glad CAM Johannsson G Korbonits M . Pseudoacromegaly: a differential diagnostic problem for acromegaly with a genetic solution . Journal of

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Nidan Qiao

transsphenoidal resection for acromegaly: a systematic review of outcomes and complications . Acta Neurochirurgica 2017 159 2193 – 2207 . ( ) 10.1007/s00701-017-3318-6 28913667 61 Monteith SJ Starke RM

Open access

Maximilian Bielohuby, Martin Bidlingmaier, and Uwe Schwahn

Bidlingmaier M. Biochemical investigations in diagnosis and follow up of acromegaly . Pituitary 2017 20 33 – 45 . ( ) 10.1007/s11102-017-0792-z 28168377 16 Braun JP Bourges-Abella N Geffre A Concordet D

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Aida Javanbakht, Massimo D’Apuzzo, Behnam Badie, and Behrouz Salehian

03346322 17598977 93 Nasr C Mason A Mayberg M Staugaitis SM Asa SL . Acromegaly and somatotroph hyperplasia with adenomatous transformation due to pituitary metastasis of a Growth Hormone-releasing hormone-secreting pulmonary endocrine carcinoma